Patient Data Reporting Videos

  1. Re-Imagining IRT For Modern Clinical Development 11/2/2023

    Get acquainted with IRT in areas such as no-code study deployment, automated excursion reviews, rapid prototyping, AI-enabled datasets, reduced (or removed) change orders, and more.

  2. ePremier: More Than A Technology Platform 10/27/2023

    Experience the unifying power of ePremier, which integrates Premier Research's data-driven processes, talented individuals, and valuable resources to drive innovation in the field of biotechnology.

  3. Medrio eConsent 10/25/2023

    Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

  4. Successful Subject Creation With eCOA, eConsent, & IRT Process Flow 5/26/2023

    Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.

  5. Efficiently Manage Clinical Data With Castor's EDC, CDMS 5/11/2023

    Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.

  6. Revolutionizing Clinical Trials: The Power Of Site-First Technology 4/20/2023

    Examine the benefits of a site-first approach to technology and consider how these tools are able to empower sites with integrated workflows that can change the clinical trial process.

  7. An ePRO Platform Designed With Real People In Mind 4/6/2023

    With a combination of technology and consultative support from team experts, start experiencing a seamless ePRO transition and establish a smoother path to regulatory submission today.

  8. Industry-First eTMF AI: PhlexTMF v21 4/6/2023

    Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.

  9. Work Flow Walk Through: eConsent Platform 2/28/2023

    Within DSG’s unified system, e-consent is simple. Witness how teams can easily and efficiently register participants for clinical trials.

  10. Medable Total Consent: The Future Of Informed Consent 2/14/2023

    With Total Consent, Medable is transforming the consenting process – harmonizing it into one simple-to-use platform that enables trial sponsors and CROs to completely customize eConsent.